Variant report

Variant	esv3351751
Chromosome Location	chr12:10472734-10522269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1124)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10519484-10519894	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:10514385-10514386	K562	blood:	n/a	n/a
3	ARID3A	chr12:10515922-10516407	K562	blood:	n/a	n/a
4	ARID3A	chr12:10517306-10518105	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:10513720-10513857	K562	blood:	n/a	n/a
6	ATF1	chr12:10518698-10519024	K562	blood:	n/a	n/a
7	ATF1	chr12:10518006-10518279	K562	blood:	n/a	n/a
8	ATF1	chr12:10515987-10516344	K562	blood:	n/a	n/a
9	ATF2	chr12:10517765-10518225	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr12:10473155-10473759	GM12878	blood:	n/a	n/a
11	ATF2	chr12:10516736-10518064	GM12878	blood:	n/a	n/a
12	ATF2	chr12:10517788-10518192	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr12:10515391-10516378	GM12878	blood:	n/a	n/a
14	ATF2	chr12:10515378-10516482	GM12878	blood:	n/a	n/a
15	ATF2	chr12:10516513-10517982	GM12878	blood:	n/a	n/a
16	ATF3	chr12:10515933-10516347	K562	blood:	n/a	n/a
17	BACH1	chr12:10517085-10517124	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr12:10516901-10517786	GM12878	blood:	n/a	n/a
19	BATF	chr12:10473160-10473741	GM12878	blood:	n/a	n/a
20	BATF	chr12:10473434-10473653	GM12878	blood:	n/a	n/a
21	BATF	chr12:10473216-10473419	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:10517007-10517370	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:10473293-10473615	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:10515491-10515913	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:10516986-10517620	GM12878	blood:	n/a	n/a
26	BCL3	chr12:10515498-10515948	GM12878	blood:	n/a	n/a
27	BCLAF1	chr12:10473313-10473710	GM12878	blood:	n/a	n/a
28	BCLAF1	chr12:10516740-10517803	GM12878	blood:	n/a	n/a
29	BCLAF1	chr12:10516330-10516752	GM12878	blood:	n/a	n/a
30	BCLAF1	chr12:10516769-10517765	GM12878	blood:	n/a	n/a
31	BHLHE40	chr12:10484273-10484556	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:10516495-10517792	K562	blood:	n/a	n/a
33	BHLHE40	chr12:10516861-10517974	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:10515999-10516244	K562	blood:	n/a	n/a
35	BHLHE40	chr12:10515601-10515915	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:10472918-10473181	GM12878	blood:	n/a	n/a
37	BRCA1	chr12:10517548-10518007	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr12:10507323-10507343	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr12:10510572-10510765	K562	blood:	n/a	n/a
40	CBX3	chr12:10515912-10516253	K562	blood:	n/a	n/a
41	CEBPB	chr12:10514223-10514644	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr12:10517667-10518134	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr12:10515495-10517606	GM12878	blood:	n/a	n/a
44	CEBPB	chr12:10474613-10474641	HepG2	liver:	n/a	n/a
45	CEBPB	chr12:10516002-10516353	K562	blood:	n/a	n/a
46	CEBPB	chr12:10516025-10516244	K562	blood:	n/a	n/a
47	CEBPB	chr12:10495834-10496064	A549	lung:	n/a	n/a
48	CEBPB	chr12:10520593-10520869	K562	blood:	n/a	n/a
49	CEBPB	chr12:10487581-10487803	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr12:10515912-10516396	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10515091-10515141	NB4	blood:	n/a
2	chr12:10515574-10515624	AoSMC	blood vessel:	n/a
3	chr12:10515091-10515141	HEK293	kidney:	embryo
4	chr12:10515574-10515624	AG04449	skin:	fetal
5	chr12:10516240-10516290	HAEpiC	amniotic membrane:	n/a
6	chr12:10515574-10515624	AG04450	lung:	fetal
7	chr12:10515574-10515624	AG10803	skin:	n/a
8	chr12:10516240-10516290	MCF-7	breast:	n/a
9	chr12:10516240-10516290	A549	lung:	n/a
10	chr12:10515574-10515624	RPTEC	kidney:	n/a
11	chr12:10515091-10515141	CMK	blood:	n/a
12	chr12:10515091-10515141	Hepatocyte	liver:	n/a
13	chr12:10515091-10515141	BE2_C	brain:	n/a
14	chr12:10516240-10516290	ECC-1	luminal epithelium:	n/a
15	chr12:10515091-10515141	AG10803	skin:	n/a
16	chr12:10515574-10515624	Caco-2	colon:	n/a
17	chr12:10515091-10515141	IMR90	lung:	fetal
18	chr12:10515091-10515141	GM12878	blood:	n/a
19	chr12:10515574-10515624	ECC-1	luminal epithelium:	n/a
20	chr12:10516240-10516290	Caco-2	colon:	n/a
21	chr12:10515574-10515624	BJ	skin:	n/a
22	chr12:10515574-10515624	HRPEpiC	eye:	n/a
23	chr12:10515091-10515141	ECC-1	luminal epithelium:	n/a
24	chr12:10516240-10516290	LNCaP	prostate:	n/a
25	chr12:10515091-10515141	GM12892	blood:	n/a
26	chr12:10515091-10515141	HCF	heart:	n/a
27	chr12:10516240-10516290	AG10803	skin:	n/a
28	chr12:10516240-10516290	BE2_C	brain:	n/a
29	chr12:10515574-10515624	HCF	heart:	n/a
30	chr12:10515091-10515141	HRE	kidney:	n/a
31	chr12:10515574-10515624	HCPEpiC	choroid plexus:	n/a
32	chr12:10515091-10515141	ProgFib	skin:	n/a
33	chr12:10515574-10515624	H1-hESC	embryonic stem cell:	embryo
34	chr12:10515574-10515624	U87	brain:	n/a
35	chr12:10515574-10515624	HCM	heart:	n/a
36	chr12:10516240-10516290	AG09319	gingival:	n/a
37	chr12:10516240-10516290	SK-N-MC	brain:	n/a
38	chr12:10515574-10515624	HIPEpiC	eye:	n/a
39	chr12:10515574-10515624	HNPCEpiC	eye:	n/a
40	chr12:10516240-10516290	HEK293	kidney:	embryo
41	chr12:10515574-10515624	SKMC	muscle:	n/a
42	chr12:10516240-10516290	HIPEpiC	eye:	n/a
43	chr12:10516240-10516290	HMEC	breast:	n/a
44	chr12:10515091-10515141	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:10515091-10515141	HCM	heart:	n/a
46	chr12:10515574-10515624	HEK293	kidney:	embryo
47	chr12:10515574-10515624	HMEC	breast:	n/a
48	chr12:10515574-10515624	GM12891	blood:	n/a
49	chr12:10515091-10515141	ovcar-3	ovarian:	n/a
50	chr12:10515574-10515624	GM12892	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10470749..10472594-chr12:10475991..10477834,2	K562	blood:
2	chr12:10483953..10484953-chr12:10826469..10827411,2	K562	blood:
3	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
4	chr12:10483978..10484906-chr12:10714545..10715159,3	MCF-7	breast:
5	chr12:10506746..10508549-chr12:10514255..10516412,2	K562	blood:
6	chr12:10436832..10439225-chr12:10509141..10511407,2	K562	blood:
7	chr12:10484283..10485072-chr12:10714510..10715568,4	K562	blood:
8	chr12:10484518..10485026-chr12:10826902..10827419,2	MCF-7	breast:
9	chr12:10519323..10520144-chr12:10902384..10903013,2	MCF-7	breast:
10	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
11	chr12:10518506..10519182-chr16:20688297..20688797,2	HCT-116	colon:
12	chr12:10484044..10484911-chr12:10711156..10712037,3	MCF-7	breast:
13	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:
14	chr12:10509675..10512643-chr12:10514341..10517366,3	K562	blood:
15	chr12:10484385..10484963-chr12:10714626..10715246,2	MCF-7	breast:
16	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-277P12.7.1-2	chr12:10485460-10485662	ENSG00000256288
2	lnc-KLRD1-1	chr12:10516368-10516632	ENSG00000245648
3	lnc-RP11-277P12.7.1-2	chr12:10490644-10490891	ENSG00000256288
4	lnc-RP11-277P12.7.1-1	chr12:10513183-10513644	ENSG00000256155
5	lnc-RP11-277P12.7.1-2	chr12:10488711-10488908	ENSG00000256288
6	lnc-RP11-277P12.7.1-1	chr12:10511063-10511162	ENSG00000256155

No data

Variant related genes	Relation type
ENSG00000256288	TF binding region
ENSG00000256155	TF binding region
ENSG00000245648	TF binding region
ENSG00000256288	CpG island
ENSG00000256155	CpG island
ENSG00000245648	CpG island
ENSG00000060140	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000256888	chromatin interactions
RNF111	miRNA target sites
LPHN2	miRNA target sites
NFIB	miRNA target sites
KIAA1967	miRNA target sites

Extended variants
information (count: 2466 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2466 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2927562	chr12:10472747-10472748	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533530912	chr12:10472759-10472760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2908448	chr12:10472765-10472766	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs2908447	chr12:10472771-10472772	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs114348566	chr12:10472801-10472802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145971645	chr12:10472813-10472814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200003251	chr12:10472862-10472863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34754455	chr12:10472863-10472864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs63208160	chr12:10472873-10472874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563517182	chr12:10472919-10472920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs3912115	chr12:10472938-10472939	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs148543836	chr12:10472973-10472974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545978229	chr12:10472982-10472983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13377899	chr12:10472984-10472985	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs183881968	chr12:10473044-10473045	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76252138	chr12:10473100-10473101	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77078706	chr12:10473253-10473254	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530691445	chr12:10473296-10473297	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148628249	chr12:10473307-10473308	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs60284246	chr12:10473320-10473321	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543342607	chr12:10473336-10473337	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562720048	chr12:10473346-10473347	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570340902	chr12:10473378-10473379	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs141161612	chr12:10473388-10473389	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546251081	chr12:10473462-10473463	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556670716	chr12:10473468-10473469	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565951085	chr12:10473469-10473470	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150712673	chr12:10473491-10473492	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554721680	chr12:10473508-10473509	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11053744	chr12:10473518-10473519	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs368932490	chr12:10473589-10473590	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139217607	chr12:10473610-10473611	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111295975	chr12:10473616-10473617	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372949636	chr12:10473658-10473659	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12309578	chr12:10473659-10473660	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs546327507	chr12:10473668-10473669	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559850219	chr12:10473694-10473695	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147593459	chr12:10473757-10473758	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573094885	chr12:10473760-10473761	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542070934	chr12:10473765-10473766	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561713821	chr12:10473776-10473777	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572803307	chr12:10473801-10473802	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530872874	chr12:10473807-10473808	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541432383	chr12:10473836-10473837	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564511662	chr12:10473895-10473896	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564119994	chr12:10473910-10473911	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532759766	chr12:10473963-10473964	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546314439	chr12:10473971-10473972	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566259820	chr12:10473979-10473980	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566538594	chr12:10473985-10473986	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1096 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10454800-10474400	Weak transcription	Left Ventricle	heart
2	chr12:10469400-10476600	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr12:10472400-10473200	Weak transcription	GM12878-XiMat	blood
4	chr12:10472400-10474000	Weak transcription	Placenta	Placenta
5	chr12:10472600-10474200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr12:10473000-10474000	Enhancers	Primary T cells from cord blood	blood
7	chr12:10473200-10474000	Enhancers	GM12878-XiMat	blood
8	chr12:10473200-10474600	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr12:10473400-10473800	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr12:10474200-10474800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:10474800-10475400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr12:10475400-10476400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:10476400-10476800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr12:10476600-10476800	Enhancers	Primary T cells fromperipheralblood	blood
15	chr12:10476800-10482600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr12:10478400-10483800	Weak transcription	Right Ventricle	heart
17	chr12:10479400-10479800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr12:10480200-10480400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr12:10480400-10488800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:10482600-10483000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr12:10483000-10484200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr12:10483000-10485400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr12:10483800-10484200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr12:10483800-10485600	Enhancers	Hela-S3	cervix
25	chr12:10484000-10485000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr12:10484200-10484400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:10484200-10484400	Enhancers	Brain Angular Gyrus	brain
28	chr12:10484200-10484600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr12:10484200-10491800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr12:10484400-10484800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:10485400-10485600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr12:10485600-10488000	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr12:10487800-10488200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:10488000-10491400	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr12:10488200-10488600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr12:10488400-10489400	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr12:10488600-10489000	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr12:10488600-10489400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr12:10488600-10489600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:10488800-10489000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr12:10489000-10489600	Active TSS	H9 Cell Line	embryonic stem cell
42	chr12:10489000-10490200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr12:10489400-10489600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr12:10489400-10490400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr12:10489400-10491400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr12:10489600-10491600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:10490200-10490600	Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr12:10490400-10490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr12:10490600-10491400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr12:10490800-10491000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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